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(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE

CAS No.
191231-58-0
Chemical Name:
(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE
Synonyms
(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE;(S)-1-Boc-2-(N-methylaminomethyl)-pyrrolidine;(S)-N-methyl-1-(1-Bocpyrrolidin-2-yl)methanamine;(S)-tert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate;tert-Butyl (S)-2-((methylamino)methyl)pyrrolidine-1-carboxylate;tert-butyl (2S)-2-[(MethylaMino)Methyl]pyrrolidine-1-carboxylate;(S)-2-[(Methylamino)methyl]-1-pyrrolidinecarboxylic acid tert-butyl ester;1-Pyrrolidinecarboxylic acid, 2-[(methylamino)methyl]-, 1,1-dimethylethyl ester, (2S)-
CBNumber:
CB5360343
Molecular Formula:
C11H22N2O2
Molecular Weight:
214.3
MDL Number:
MFCD07786221
MOL File:
191231-58-0.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:44
Product description Number Pack Size Price
(S)-tert-Butyl2-((methylamino)methyl)pyrrolidine-1-carboxylate B814795 10mg $45
(S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate FB142890 250mg $250
(S)-Tert-butyl2-((methylamino)methyl)pyrrolidine-1-carboxylate 8504BB 250mg $323
(S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate FB142890 500mg $405
(S)-1-Boc-2-(methylaminomethyl)pyrrolidine 95% ee AS101610 1g $458

(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE Properties

Boiling point 282℃
Density 1.004
Flash point 124℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 10.17±0.10(Predicted)
Appearance Colorless to light yellow Viscous Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B814795 (S)-tert-Butyl2-((methylamino)methyl)pyrrolidine-1-carboxylate 191231-58-0 10mg $45 2021-12-16 Buy
Biosynth Carbosynth FB142890 (S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate 191231-58-0 250mg $250 2021-12-16 Buy
AK Scientific 8504BB (S)-Tert-butyl2-((methylamino)methyl)pyrrolidine-1-carboxylate 191231-58-0 250mg $323 2021-12-16 Buy
Biosynth Carbosynth FB142890 (S)-tert-Butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate 191231-58-0 500mg $405 2021-12-16 Buy
Activate Scientific AS101610 (S)-1-Boc-2-(methylaminomethyl)pyrrolidine 95% ee 191231-58-0 1g $458 2021-12-16 Buy
Product number Packaging Price Buy
B814795 10mg $45 Buy
FB142890 250mg $250 Buy
8504BB 250mg $323 Buy
FB142890 500mg $405 Buy
AS101610 1g $458 Buy

(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE Chemical Properties,Uses,Production

Synthesis

N-Allylmethylamine

627-37-2

BOC-L-Prolinol

69610-40-8

(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE

191231-58-0

The general procedure for the synthesis of tert-butyl (S)-2-((methylamino)methyl)pyrrolidine-1-carboxylate from N-methylallylamine and N-BOC-L-prolinol was as follows: Boc-L-prolinol (6.03 g, 30 mmol) was dissolved in anhydrous DCM (120 mL), TEA (15 mL) and anhydrous DMSO (33 mL) were added. Subsequently, PyrSO3 powder (total 30 g) was added in batches of 5 g each for 2 h until the LCMS assay showed complete consumption of raw alcohol. The reaction mixture was washed sequentially with 6N NaHSO4 (3 × 100 mL) and water (2 × 100 mL) and then transferred to a flask. To the flask was added N-methylallylamine (2.8 mL, 29 mmol) followed by NaBH(OAc)3 (6.36 g, 30 mmol). After stirring for 30 min, the mixture was transferred to a partition funnel, the organic layer was washed with water (100 mL), dried and concentrated to give an oily product (4.5 g). This oily product was dissolved in THF (100 mL) and bubbled with N2 gas for 10 minutes. Thiosalicylic acid (4.1 g, 26.6 mmol), Pd2dba3 (137 mg, 0.5 mmol) and 1,4-bis(diphenylphosphino)butane (128 mg, 0.30 mmol) were added. The reaction mixture was sealed and stirred for 1 h at room temperature and then concentrated. It was washed sequentially with 4N NaOH (2 x 50 mL) and water (50 mL), dried and concentrated to give a red oily material. This oily material was stirred with hexane (200 mL) for 10 min, the hexane layer was separated and concentrated to give the target product (3.0 g).MS (M + 1)+: 215.2.

References

[1] Patent: WO2017/3724, 2017, A1. Location in patent: Paragraph 00214

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(S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE Spectrum

(S)-N-methyl-1-(1-Bocpyrrolidin-2-yl)methanamine (S)-tert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate tert-butyl (2S)-2-[(MethylaMino)Methyl]pyrrolidine-1-carboxylate (S)-2-[(Methylamino)methyl]-1-pyrrolidinecarboxylic acid tert-butyl ester (S)-1-BOC-2-(METHYLAMINOMETHYL)-PYRROLIDINE (S)-1-Boc-2-(N-methylaminomethyl)-pyrrolidine 1-Pyrrolidinecarboxylic acid, 2-[(methylamino)methyl]-, 1,1-dimethylethyl ester, (2S)- tert-Butyl (S)-2-((methylamino)methyl)pyrrolidine-1-carboxylate 191231-58-0