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(R)-(+)-1-Boc-3-aminopyrrolidine → HCID 178452029, compound

HRID 2017650
Notes
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Reaction equation

HRID 2017650 reaction equation
[CH3:1][C:2]([O:5][C:6]([N:8]1[CH2:13][C@H:11]([NH2:12])[CH2:10][CH2:9]1)=[O:7])([CH3:4])[CH3:3].Br[c:14]1[n:22][c:21]([c:17]2[cH:16][cH:15]1)[cH:20]c[cH:19][c:18]2[C:23]#[N:24]>>[CH3:1][C:2]([O:5][C:6]([N:8]1[CH2:13][C@H:11]([NH:12][c:17]2[cH:23][n:24][c:14]([N:22]3[CH2:19][CH2:18]O[CH2:20][CH2:21]3)[cH:15][cH:16]2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])[CH3:3]
ParticipantsConditionsSources & evidenceReaction notes

Participants

7

Reactant 2

HCID 854070(R)-(+)-1-Boc-3-aminopyrrolidineHCID 121410810HCID 121410810, compound

Product 1

HCID 178452029HCID 178452029, compound

Reagents, catalysts & solvents 4

HCID 23683543Potassium t-amylateReagentHCID 178492617HCID 178492617, compoundCatalystHCID 312751,4-DioxaneSolvent

Conditions

Temperature
120 °C

Sources & evidence

ORD record
ord-2e5e70c64b5d47c5960902614c01eb01
Source dataset
39k HTE dataset from Pfizer
DOI
10.1038/s41557
Original link
View source

Reaction notes

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On this pageParticipantsConditionsSources & evidenceReaction notes
HCID 117669-PhenylanthraceneInternal standard